A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579127



Internal ID16366536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27287920..27783601hg38UCSC Ensembl
Innerchr19:27778828..28274509hg19UCSC Ensembl
Innerchr19:32470668..32966349hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38495682
hg19495682
hg18495682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv897037
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579127
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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